ProfileGDS1065 / 221428_s_at
TitleMitochondrial encephalomyopathies associated with mitochondrial DNA mutations
OrganismHomo sapiens


wild type A3243G large deletion normal MELAS PEO GSM24652 GSM24653 GSM24654 GSM24655 GSM24656 GSM24657 GSM24658 GSM24659 GSM24660 GSM24661 GSM24662 GSM24663 GSM24664 GSM24665 GSM24666 38% 29% 60% 37% 56% 15% 28% 27% 39% 26% 21% 28% 57% 65% 58% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 126.438
GSM24653Normal subject 215.629
GSM24654Normal subject 383.660
GSM24655A3243G-MELAS subject 119.237
GSM24656A3243G-MELAS subject 259.856
GSM24657A3243G-MELAS subject 38.415
GSM24658A3243G-MELAS subject 412.828
GSM24659A3243G-PEO subject 113.627
GSM24660A3243G-PEO subject 226.139
GSM24661A3243G-PEO subject 39.126
GSM24662A3243G-PEO subject 48.421
GSM24663mtDNA "Common"-deletion subject 114.828
GSM24664mtDNA "Common"-deletion subject 2106.557
GSM24665mtDNA "Common"-deletion subject 3121.565
GSM24666mtDNA "Common"-deletion subject 494.458